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Biomedical subjects

F Fakan

Publications and source records attributed to F Fakan.

At least 37 records · Page 2Linked to original sources

[Primary cutaneous B-cell lymphoma: present views].

Most lymphoproliferative B cell cutaneous lesions do represent primary lymphomas, not a secondary lymphomatous spread or pseudolymphoma* A description of the development of classification systems for primary cutaneous B lymphomas is given concerning especially some newly defined lesions: primary cutaneous marginal zone B cell lymphoma, primary cutaneous follicular centre cell lymphoma and large B cell lymphoma of the legs. Majority of primary cutaneous B lymphomas answer well the treatment and have a favourable prognosis.

Humans↗

Liver cell cytoplasmic inclusions in experimental porphyrias: their demonstration with the ferric ferricyanide reduction reaction.

In the present paper we describe needle-shaped and granular cytoplasmic inclusions in the liver cells of mice and rats with experimental porphyria biochemically resembling human porphyria cutanea tarda. The inclusions were inconspicuous in routine histological slides. The ferric ferricyanide reduction reaction, however, enabled us to demonstrate their shape and location within the hepatic lobule. Needle-shaped inclusions are considered to represent a structure specifically seen in experimental porphyrias resembling porphyria cutanea tarda. These structures are similar to the inclusions seen in human porphyria cutanea tarda.

Animals↗

[The ferricyanide reduction reaction as a staining method in liver biopsy].

In paraffin sections from human liver tissue, ferric ferricyanide reduction reaction enables to visualize various reducing substances. Firstly it is cholestasis due to reduction capacity of bilirubin. Another reducing substance is lipofuscin pigment. Finally, the reaction represents the only way to demonstrate the needle-shaped cytoplasmic inclusions in routine practice considered to be specific for porphyria cutanea tarda. The method is simple and inexpensive and it may be recommended as a suitable supplementary staining procedure for liver biopsies.

Biopsy↗

[Monoclonal plasmacytic differentiation in small-cell lymphomas of B-cell origin: immunocytoma versus other types].

We have studied the morphological and immunohistochemical features of monoclonal cytoplasmic Ig (c-Ig) production in the biopsy material of 161 small B-cell non-Hodgkin's lymphomas to verify a frequency of the plasmacytic/plasmacytoid differentiation of tumor cells for the aims of their differential diagnosis. The analyzed differentiation was identified in all the cases of immunocytoma (n = 20/20), in 2/3 of MALT-lymphomas (n = 24/38) and 1/2 of monocytoid B-cell lymphoma cases (n = 4/7), in 1/5 of centroblastic-centrocytic lymphoma cases (n = 12/60) and rarely in centrocytoma (n = 4/36). We conclude that a plasmacytic differentiation is not an unique feature of the immunocytoma. For the differential diagnosis, a histological analysis and not a proof of monoclonal c-Ig itself seems to be decisive. The obtained results are discussed in relation to the histogenesis of small B-cell lymphomas, which represent a neoplastic counterpart of the reactive B-cells at different stages of their maturation and differentiation.

Diagnosis, Differential↗

[Multiple lymphomatous polyposis of the gastrointestinal tract].

We studied three patients in whom histology revealed multiple lymphomatous polyposis of the gastrointestinal tract. It is a distinctive type of primary gastrointestinal lymphoma characterized by polypoid accumulations of lymphoma tissue involving long segments of the gastrointestinal tract. This lymphoma consists of a diffuse proliferation of small round lymphocytes and small cleaved cells and tends to an extraintestinal dissemination. Clinical behavior of this entity is more aggressive than that of the same primary nodal lymphoma. We discuss the evolution of opinions of this entity.

Aged↗

Carcinoma arising in ectopic hamartomatous thymoma. An ultrastructural study.

We present the ultrastructural features of a case of adenocarcinoma arising in ectopic hamartomatous thymoma in a 31 year old man, in the supraclavicular location. The tumor had a cribriform adenomatous component with a granular cell quality and mimicked a metastatic carcinoma. Ultrastructurally, the spindle cell component revealed clusters of tonofilaments and the tumor cells were attached by well developed desmosomes. The cytoplasm of adenocarcinoma cells contained peculiar cup-shaped bodies derived from the endoplasmic reticulum wrapped around the mitochondria.

Adenocarcinoma↗

Expression of bcl-2 protein in distinguishing benign from malignant lymphoid aggregates in bone marrow biopsies.

In this study, the immunohistochemical expression of bcl-2 protein in benign and malignant lymphoid aggregates in bone marrow biopsies was investigated in order to estimate its significance in distinguishing the biologic nature of the aggregates. Paraffin-embedded tissues of 46 bone marrow biopsies were stained with a monoclonal antibody to bcl-2 protein using the supersensitive streptavidin biotin immunoperoxidase method after a microwave heating of the sections. Bcl-2 protein immunoreactivity was observed in various proportions of lymphoid cells in both reactive and malignant lymphoid bone marrow aggregates. The percentage of bcl-2 positive cells in malignant aggregates was substantially higher (mean value 78%) than that observed in reactive nodules (mean value 60%). The presence of bcl-2 protein has been confirmed both in malignant and benign bone marrow lymphoid aggregates. Thus, the bcl-2 protein expression should not be used as a discriminating criterion for the malignant nature of lymphoid aggregates.

Biomarkers, Tumor↗

[Chondroid lipoma].

Chondroid lipoma had not been defined until 1993. Here presented case was a 30-year old woman with a well limited soft tissue tumour of the left thigh. In histology, the encapsulated tumour consisted of mature adipocytes in common lipoma like areas and of a chondroid component in which lipoblastic or hibernoma like cells were surrounded by a myxohyaline matrix. Both components were connected and mutually transient. Tumour cells showed S-100 protein and laminin positivity in immunohistochemistry. Cells of the chondroid component had distinct ultrastructural features of adipose and cartilagineous differentiation. Chondroid lipoma is a benign tumour which is to be distinguished from extraskeletal myxoid chondrosarcoma and myxoid liposarcoma.

Adult↗

[Segmental mediolytic arteriopathy].

Three cases of segmental mediolytic arteriopathy occurring in abdominal muscular arteries are presented. This unusual arterial lesion is noted for cytoplasmic vacuolar degeneration of the arterial smooth muscle cells, intercellular vacuoles of various sizes, and focal arterial wall defects designated "arterial gaps". This spectrum of histologic changes can progress to formation of aneurysms with rupture of the vascular wall. The extensive intraabdominal haemorrhage led to the death of all our patients. Pathogenesis and differential diagnosis of this lesion is discussed.

Aged↗

Nodular transformation of splenic red pulp due to carcinomatous infiltration. A diagnostic pitfall.

Autopsy of three women dying of disseminated carcinoma of stomach, colon, and breast, respectively, revealed a grossly unremarkable spleen. Microscopic examination demonstrated a nodular transformation of the red pulp, simulating a follicular lymphoma. Immunostaining revealed dissociated carcinomatous cells between the nodules, and this was thought to be the cause of the nodular transformation.

Aged↗

[Anaplastic Ki-1/CD30 positive lymphoma].

Ki-1(CD30) positive lymphoma in its large cell variant represents a distinct histopathological entity. Its cells have a characteristic morphology, immunophenotype and karyotype. In the beginning the tumour infiltrates sinuses of the lymph node and it can be difficult to distinguish it from a metastatic carcinoma or melanoma. We present here six cases of this peculiar entity.

Aged↗

[T-lymphocyte-rich large B-cell lymphoma--case report].

A 60-year-old man presented with hepatosplenomegaly and signs of hepatic failure. The patient underwent splenectomy and liver biopsy. Histologic sections of the liver and the spleen showed nodular infiltrates composed of scattered large atypical cells that resembled Sternberg-Reed (SR) cells intermingled with abundant small T-lymphocytes. Large atypical cells showed B phenotype (CD20 positivity) and did not express CD15 and CD30 antigens typical of SR cells.

Antigens, CD↗

[Fixation and decalcification in trephination biopsy].

We tested several modifications of paraffin embedding technique when examining bone marrow biopsies in order to achieve an optimal combination of morphology and antigen preservation. Short pre-fixation in formalin followed by mixture of formalin and 10% formic acid were found optimal for quick tissue processing where electron microscopy was not planned. Formalin pre-fixation prevents the occurrence of imperfect stainability of superficial parts of trephine cylinders caused by an effect of formic acid on non-fixed bone marrow tissues. Decalcification in mixture of formol and EDTA is recommended if there is time enough. The supersensitive streptavidin-biotin detection system with alkaline phosphatase was found to provide the best results.

Biopsy↗

[Bimorphic malignant lymphoma].

Two distinct morphological types of malignant lymphoma in the same patient occur mostly due to transformation of a low-grade lymphoma to high-grade lymphoma. When two morphologically different structures are found at different sites they represent discordant lymphoma. Composite lymphoma, on the other hand, shows two histologic subtypes involving the same location. Bimorphic morphology of malignant lymphoma is of therapeutic and prognostic significance.

Hodgkin Disease↗

Littoral cell angioma of the spleen. A case report with ultrastructural and immunohistochemical observations.

We describe histological, immunohistochemical and ultrastructural findings in a case of littoral cell angioma of the spleen in a 44 year old man. Beside phagocytosis and heavy haemosiderin deposits in the cytoplasm, a very characteristic and hitherto undescribed feature of the littoral cells was focal accumulations of eosinophilic globules 0.5-2 microns in size, which often entirely filled the cytoplasm of the tumour cells. Ultrastructurally the globules were composed of abundant cytoplasmic deposits of lysosomes and residual bodies. The globules most probably originate from the phagocytized red blood cells, lymphocytes and plasma cells. Immunohistochemically the tumour cells reacted positively with antibodies against factor VIII-related antigen, KiM1P, KP1 and lysozyme and negatively with antibodies against cytokeratins AE1-AE3, EMA and S-100 protein. Ultrastructurally the tumour cells often formed long cytoplasmic processes without external lamina and pinocytic vesicles. Scarce and poorly formed junctions between the tumour cells were seen. Very rarely cytoplasmic rod-shaped microtubulated bodies, often difficult to distinguish from heavy accumulations of lysosomes were observed.

Adult↗

Palisaded intranodal myofibroblastoma. Electron microscopic study.

Described in this paper are the ultrastructural features of three cases of palisaded intranodal myofibroblastoma. The tumor cells were identified as myofibroblasts. Abortive vessels formed by the tumor in one case and spindle cell tumorous proliferation outside the tumor capsule and centered on the veins were composed of the same cell types as the cells of the main tumor mass, suggesting that the tumorous myofibroblasts might have originated from the modified smooth muscle cells. The various stages of formation of the intracytoplasmic fuchsinophilic bodies are described in our report.

Collagen↗